Partnering Solutions

  1. A CRO Accelerating Bioanalysis 9/8/2025

    Move drug development into the modern era with a CRO that offers assay development and validation, bioanalytical testing, sample prep, and more.

  2. Biorasi Rare and Urgent Disease 9/21/2021

    Read how Biorasi's speed and agility make all the difference in overcoming unique obstacles to rare disease clinical trials.

  3. Gene Therapy Ready Site Network 4/5/2022

    Join more than 1,000 research sites who use Advarra as their IBC of record. Is your research site ready to take advantage of this growing area of clinical trials?

  4. Integrated CRO Services 1/26/2023

    With over 30 years of experience, Altasceinces delivers customized and scalable CRO services purpose-built for early-phase to Phase Ib/IIa development.

  5. USP 661.1 Vs 661.2: Key Differences And Compliance 1/9/2026

    USP 661.1 and 661.2 introduce rigorous, risk-based standards for pharmaceutical plastic packaging, emphasizing material characterization, system suitability, and extractables/leachables testing to ensure safety and compliance.

  6. Transforming Clinical Trial Site Forecasting 10/30/2024

    In today’s ever-evolving clinical trial space, managing the expenses associated with conducting a study is more important – and fraught – than ever before.

  7. Central Nervous System Drug Development 1/16/2026

    CNS drug development faces unique hurdles — from high placebo response to complex protocols and recruitment challenges. Discover strategies to streamline trials, optimize planning, and accelerate delivery of innovative therapies for patients with critical unmet needs.

  8. SMART First Human Dose (FHD)

    A CDMO with the right team of experts can aid drug development, regulatory compliance, and clinical trial supply, accelerating timelines to first human dose clinical trials and the path to market.

  9. An Introductory Guide To Clinical EU Qualified Person (QP) Services 10/3/2022

    PCI's team of qualified persons assume responsibility for all stages of the process, safeguarding patients including the audit of the supply chain for GMP compliance in addition to certification of products for use in clinical trials.

  10. Greenphire Clinical Finance: Budgeting & Benchmarking 10/23/2025

    Streamline trial budgets and payments with real-time fair market data, speeding startups and ensuring timely, transparent site funding worldwide.